cycad anatomy and fossil occurrences in texas · 2017-10-18 · thought they were a common...

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CYCAD ANATOMY AND FOSSIL OCCURRENCES IN TEXAS By Scott Singleton Houston Gem and Mineral Society ([email protected]) ycadophyta presently consists of the living order Cycadales, which is comprised of three families worldwide. In the Mesozoic, cycads were represented by the Cycadales, plus another large order, Cycadeoidales (also referred to as Bennettitales). Cycadophyta is thought to have evolved from the Paleozoic seed ferns (pteridosperms), as did conifers, and eventually, angiosperms. However, Cycadales and Cycadeoidales likely arose from two distinct forms of pteridosperms. Their similarity is thought to be the result of convergent and/or parallel evolution (Norstag & Nicholls, 1997). Cycadeoid remains are much more prevalent in the fossil record, and thus it is thought they were a common constituent of the plant assemblage. (Conversely, Cycadales are relatively rare in the fossil record). Ultimately, Cycadeoids became extinct by the end of the Cretaceous. One theory postulates that they were dependent on specific insects to spread their pollen from plant to plant because the female ovule was completely encapsulated within the cone, and that for some reason they lost their insect-pollinators (Norstag & Nicholls, 1997). However, others feel that the Cycadales had evolved a slightly more advanced megaspore and ovule structure, thus allowing them to survive into the Tertiary whereas many other organisms, including dinosaurs, failed to adjust to the changes at the end of the Cretaceous (Tidwell, pers. comm.). C “The two orders are very similar, particularly with respect to general growth habit and leaf organization. Trunks of both orders range from short and squat [Figure 2] to tall and columnar [Figure1] and are covered by a protective layer of leaf bases that persist after the leaves drop off…The basic difference between [the two is that] cones occur at the apex [top] of the stem [in] living cycads [Figure 1], but are embedded among the leaf bases in cycadeoids [Figures 2-5]” (Tidwell, 1998). There are other primary differences that set cycadeoids well apart botanically from the Cycadales, such as the method of origination of leaf bases within the trunk and the cellular configuration of leaf epidermis. 1

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Page 1: CYCAD ANATOMY AND FOSSIL OCCURRENCES IN TEXAS · 2017-10-18 · thought they were a common constituent of the plant ... Notes on some Fossil Plants from the Trinity Division of the

CYCAD ANATOMY AND FOSSIL OCCURRENCES IN TEXAS

By Scott Singleton Houston Gem and Mineral Society

([email protected])

ycadophyta presently consists of the living order Cycadales, which is comprised of three families worldwide. In the Mesozoic, cycads were represented by the Cycadales, plus another large order, Cycadeoidales (also referred to as

Bennettitales). Cycadophyta is thought to have evolved from the Paleozoic seed ferns (pteridosperms), as did conifers, and eventually, angiosperms. However, Cycadales and Cycadeoidales likely arose from two distinct forms of pteridosperms. Their similarity is thought to be the result of convergent and/or parallel evolution (Norstag & Nicholls, 1997). Cycadeoid remains are much more prevalent in the fossil record, and thus it is thought they were a common constituent of the plant assemblage. (Conversely, Cycadales are relatively rare in the fossil record). Ultimately, Cycadeoids became extinct by the end of the Cretaceous. One theory postulates that they were dependent on specific insects to spread their pollen from plant to plant because the female ovule was completely encapsulated within the cone, and that for some reason they lost their insect-pollinators (Norstag & Nicholls, 1997). However, others feel that the Cycadales had evolved a slightly more advanced megaspore and ovule structure, thus allowing them to survive into the Tertiary whereas many other organisms, including dinosaurs, failed to adjust to the changes at the end of the Cretaceous (Tidwell, pers. comm.).

C

“The two orders are very similar, particularly with respect to general growth habit and leaf organization. Trunks of both orders range from short and squat [Figure 2] to tall and columnar [Figure1] and are covered by a protective layer of leaf bases that persist after the leaves drop off…The basic difference between [the two is that] cones occur at the apex [top] of the stem [in] living cycads [Figure 1], but are embedded among the leaf bases in cycadeoids [Figures 2-5]” (Tidwell, 1998). There are other primary differences that set cycadeoids well apart botanically from the Cycadales, such as the method of origination of leaf bases within the trunk and the cellular configuration of leaf epidermis.

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Page 2: CYCAD ANATOMY AND FOSSIL OCCURRENCES IN TEXAS · 2017-10-18 · thought they were a common constituent of the plant ... Notes on some Fossil Plants from the Trinity Division of the

Figure 1: Cycadalean structure (from Figure 2: Cycadeoidalean structure Tidwell, 1998). (from Tidwell,1998)

Figure 3: Cycadeoid trunk showing cones Figure 4: Cycadeoid tangential section and leaf bases (from Wieland, 1916). 4 cm from exterior of trunk showing leaf

bases and a cone (from Wieland, 1906).

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Figure 5: Yale University cycadeoid collection from the Black Hills of South Dakota (from Wieland, 1916). Interestingly enough, from a distance cycads look something like small palm trees with stout stems because of the persistent leaf bases on the exterior of the trunk and the crown of spirally-arranged compound leaves. Because of this similarity, a cycad imported from the Far East and used as a potted and landscape plant in the Southern U.S. has been given the common name “Sago Palm”! Cycad Anatomy: In transverse section, the stele (or trunk) of Cycadales and cycadeoids has a large central pith (or medulla) surrounded by a broad ring of vascular tissue composed of secondary xylem and secondary phloem dissected by wide rays (Figures 6 and 7). The secondary xylem is composed of a high percentage of parenchyma among the normal tracheid cells (called manoxylic). This is followed by a cortex and then an outer “armor” that is composed of ramentum (described below), leaf bases, and (in cycadeoids) cones (Figures 6 and 7). Both the pith and the cortex can contain secretory canals (Figure 7). Leaf traces in the cortex appear as a C-shaped bundle (Figure 6), similar to fern leaf traces.

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Figure 6: Transverse section through the Figure 7: Transverse section through the upper portion of a cycadeoid trunk with mid-section of a cycadeoid trunk showing anatomical features identified (from pith (p), secondary xylem (sx), and a Wieland, 1906). thick armor consisting of ramentum (r),

leaf bases (lb), and cone (c). Cortex is thin and is between secondary xylem and ramentum (from Stewart and Rothwell, 1993).

The outer armor of a cycad trunk consists of leaf bases that remain after the leaf dies and falls off. Leaf bases appear rhombohedral in cross section and give cycad trunks their distinctive look (Figures 2, 3, and 4). On the exterior of the trunk between the leaf bases is a dense packing of ramentum, which can either be long, scaly hairs or flat, tongue-shaped scale-like structures known as cataphylls. Their purpose is entirely one of protection. As they age, they may lose their tips and become embedded between leaves. Thus, cycad trunk armor may be half ramentum (by volume), densely packed between the leaf bases and, in cycadeoids, the cones. Cycadeoid cones appear on the exterior of the trunk as a circular mass surrounded by small leaf traces (Figures 3 and 4). In cross-section, cones extend through the entire armor section, opening their distal end to the outside upon maturity (Figure 7). The cones themselves contain the pollen and seed producing structures (Figures 8 and 9), and are often seen in exquisite detail in fossil specimens. The presence of cones in the armor section of a fossil cycad positively identifies it as a cycadeoid rather than Cycadalean. For instance, the popular Patagonian (Argentina) cycads are Jurassic in age and show obvious cones, thus they are cycadeoids.

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Figure 8: Longitudinal section through Figure 9: Longitudinal section through ovulate ovulate cone of a cycadeoid. This cone cone of a cycadeoid. This cone is young and is mature and shows developed seeds is only starting to develop ovules (3x) (from (10x) (from Wieland, 1916). Wieland, 1916). The stem morphology of cycad trunks varies considerably depending on the species as well as on the vertical position in the trunk. A thick armor made up of leaf bases and ramentum is likely in the lower sections, thinning upward toward the apical meristem (growth tip). The secondary xylem is also likely to be thicker in lower portions which have undergone multiple years of annual growth (Figure 10). The cortex is likely to be developed in the upper portions where new growth is prominent. The pith is present through the entire stem (Figures 10 and 11), but both the cortex and the pith are less dense (more spongy) than either the secondary xylem or armor. During growth this can lead to either being squeezed or compressed, and compressive stresses during fossilization can lead to a considerable reduction in volume of both. (Note that on many of the illustrations in this text the cortex is either thin or not visible).

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P

SX

A

P

SX

A

Figure 10: Transverse section through the Figure 11: Transverse section through base of a Cycadeoidea jenneyana trunk the mid region of a Cycadeoidea showing a small pith (P), thick secondary stillwelli trunk showing substantial pith xylem (SX), and an armor section (A) that (P), minimal secondary xylem (SX), and has been mostly eroded away (from a thick armor (A) (from Wieland, 1916). Wieland, 1906).

Occurrence in Texas: Both cycads and cycadeoids occur in Texas, although they are not common or widely reported. Fontaine (1893) described an abundance of cycad, conifer, and fern leaves from the Glen Rose Formation, Lower Cretaceous (Trinity Group), two miles up the Paluxy River from the town of Glen Rose. His specimens were from limestone that he judged was deposited some distance from shore. He did not, however, mention any cycad trunks (or any wood) being found. Wieland (1931), the well-regarded early researcher in fossil cycads, described a visit to Stephenville where, through the courtesy of a number of devoted rockhounds, he obtained numerous cycadeoid trunks for the U.S. National Museum at Yale. Wieland identified and named five distinct species. The specimens were collected from a variety of locations, but all were from the lowest Cretaceous Trinity Group. Based on current nomenclature, the localities (and formations in parentheses) are, from north to south (Figure 12):

• Bridgeport, Wise County (Antlers Sand or Twin Mountains)

• Tolar, Hood County (Paluxy Sand)

• Stephenville, Erath County (Paluxy Sand)

• Comanche, Comanche County (Twin Mountains)

• Fredericksburg, Gillespie County (Hensell Sand)

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Figure 12: Locations where cycads have been found in Texas. Five-sided stars are Early Cretaceous localities; 4-sided star is Tertiary cycad site. Map courtesy of the U.S. Census Bureau (http://quickfacts.census.gov/qfd/maps/). Cycads occur in the Tertiary of Texas, in a region of the central Gulf Coast encompassing Karnes, Live Oak, and McMullen Counties (although the actual extent may be larger). There is some uncertainty surrounding the actual age of these cycads. They occur in the George West area (Goliad Formation, Miocene, Figure 12), and I have heard reports that they occur in the prolific Manning Formation (Upper Eocene Jackson Group). However, I have not personally verified the Manning Formation reports. Compounding this issue, the Goliad Formation in the George West area is problematic. These caliche-impregnated sediments are derived from the paleo-Nueces River and floodplain. Many (but not all) of the specimens are rounded, indicating they have undergone transport and weathering at some time in the past. Thus, they may or may not represent in-situ material, and therefore may or may not be derived from Miocene age plants. It is apparent that further research and documentation is needed on these fossil remains.

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PP

SX

LB

LB

LB

LB

Figure 13: One quarter section of a fossil cycad from George West, Live Oak County (Goliad Formation, Miocene). Although very mineralized, several anatomical features are present [pith (P), secondary xylem (SX), leaf bases (LB)]. The outer portion of the trunk was missing due to weathering. Specimen is 5” across from left to right. (Singleton Collection) Figure 13 shows a section of a George West fossil cycad. This specimen is from a sizable cycad trunk. Prior to slicing, it was about 6” in diameter and 10” tall, and the diameter only represented about ¼ of the trunk. The remainder had undoubtedly broken off due to natural fracturing and weathering. Mineralization is substantial, which is typical for material from that area. Despite this, basic anatomical features of a cycad can be seen, including the pith, secondary xylem, and several leaf bases. Possibly due to the extensive mineralization, the cortex section is not apparent. However, the armor section is identifiable by the presence of several leaf bases.

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Acknowledgements I’d like to thank Dr. William Tidwell for permission to use Figures 1 and 2, and for his helpful discussions and technical review of this paper. References Fontaine, W.M., 1893, Notes on some Fossil Plants from the Trinity Division of the Comanche Series of Texas, Proceedings of the U.S. National Museum, Vol. XVI, p. 261-282. Norstag, K.J., and T.J. Nicholls, 1997, The Biology of the Cycads, Cornell University Press, Ithica, NY, and London, UK. Stewart, W.N., and G.W. Rothwell, 1993, Paleobotany and the Evolution of Plants, 2nd ed., Cambridge University Press, Cambridge, UK. Tidwell, W.D., 1998, Common Fossil Plants of Western North America, 2nd ed., Smithsonian Institution Press, Washington, DC. Wieland, G.R., 1906, American Fossil Cycads, Carnegie Institution of Washington, Washington, DC. Wieland, G.R., 1916, American Fossil Cycads, Volume II, Carnegie Institution of Washington, Washington, DC. Wieland, G.R., 1931, Land Types of the Trinity Beds, Science, Vol. 74, No. 1920, p. 393-395.

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